CNR Institutional Research Information System

QUATTRONE, ALDO
 Distribuzione geografica
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Continente #
AS - Asia 83
EU - Europa 29
NA - Nord America 25
Totale 137
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Nazione #
CN - Cina 47
KR - Corea 36
US - Stati Uniti d'America 25
IT - Italia 23
FR - Francia 2
NL - Olanda 2
DE - Germania 1
SE - Svezia 1
Totale 137
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Città #
Seoul 36
Boardman 21
Guangzhou 9
Capua 5
Amsterdam 2
Canelli 2
Capaccio 2
Forest City 2
Milan 2
Paris 2
Reggio Calabria 2
Bovalino 1
Cerisano 1
Cittaducale 1
Montesilvano Marina 1
New York 1
Pontedera 1
Totale 91
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Nome #
An SNP site in pri-miR-124, a brain expressed miRNA gene, no contribution to mesial temporal lobe epilepsy in an Italian sample 3
ASSOCIATION OF A GABA(B) GENE HAPLOTYPE AND TEMPORAL LOBE EPILEPSY 3
A New MRI Measure to Early Differentiate Progressive Supranuclear Palsy From De Novo Parkinson's Disease in Clinical Practice: An International Study 2
The motor inhibition system in Parkinson's disease with levodopa-induced dyskinesias. 2
Altered cortical-cerebellar circuits during verbal working memory in essential tremor 2
A comprehensive mutation analysis of PINK1 gene in South Italy patients with early and late onset Parkinsonism. 2
A Fully Automated, Atlas-Based Approach for Superior Cerebellar Peduncle Evaluation in Progressive Supranuclear Palsy Phenotypes. 2
Exosome-associated miRNA profile as a prognostic tool for therapy response monitoring in multiple sclerosis patients. 2
Comparison of different techniques for detecting 17p12 duplication in CMT1A. 2
A CNN Based Algorithm for the Automated Segmentation of Multiple Sclerosis Lesions 2
A longitudinal evaluation of cadasil progression by diffusion magnetic resonance imaging. 2
Novel spastin (SPG4) mutations in Italian patients with hereditary spastic paraplegia 2
A Cellular Neural Network methodology for the automated segmentation of multiple sclerosis lesions 2
A CLINICAL AND MOLECULAR STUDY IN A CHILD UNDER 1 YEAR OF AGE AFFECTED BY NEUROFIBROMATOSIS TYPE 2 2
The effectiveness of cognitive treatment in patients with Parkinson's disease: A new phase for the neuropsychological rehabilitation. 2
A novel NOTCH3 gene mutation in a patient with CADASIL from Southern Italy 2
A Functional Genetic Variation of the 5-HTR2A Receptor Affects Age at Onset in Patients with Temporal Lobe Epilepsy. 2
'The syphilitic' by Albrecht Dürer (1471-1528). 2
Value of Clinical Features to Differentiate Refractory Epilepsy from Mimics A prospective longitudinal cohort study. 2
A novel founder mutation in the MFN2 gene associated with variable Charcot-Marie-Tooth type 2 phenotype in two families from Southern Italy. 2
Author's reply to the comment of Sironi et al. on "Compound heterozygosity in DJ-1 gene non-coding portion related to Parkinsonism" 2
A novel Notch3 gene mutation not involving a cysteine residue in an Italian family with CADASIL. 2
Refining initial diagnosis of Parkinson's disease after follow-up: A 4-year prospective clinical and magnetic resonance imaging study. 2
Adaptive cortical changes and the functional correlates of visuo-motor integration in relapsing-remitting multiple sclerosis 2
Opicapone-induced reversible myopathy in a patient with advanced Parkinson's disease and familial hyperCKemia 2
MRI measures of brainstem in Parkinsonian syndromes: Where we stand and where we need to go 2
A new locus for autosomal dominant nocturnal frontal lobe epilepsy maps to chromosome 1 2
Dropped head syndrome in a patient with FTD-ALS caused by abnormal expansion of C9orf72 gene. 1
Multiple system atrophy and C9orf72 hexanucleotide repeat expansions in a cohort of Italian patients 1
A SLC20A2 mutation identified in an asymptomatic patient with brain calcification 1
Alpha synuclein in familial parkinson s disease and lewy body dementia. 1
Gene Symbol: MECP2. Disease: Rett Syndrome. 1
Reduced Striatal DAT Uptake Normalizes After Shunt in Normal-Pressure Hydrocephalus 1
Alpha-synuclein promoter haplotypes and dementia in Parkinson's disease. 1
Clinical and genetic study of an Italian family linked to SPG26 locus 1
A family with dominant optic atrophy and deafness due to a novel Opa1 mutation. 1
Blink re fl ex recovery cycle distinguishes essential tremor with resting tremor from de novo Parkinson ' s disease: An exploratory study 1
A Clinical And Molecular Study In Children Under 1 Year Of Age Affected By Neurofibromatosis Type 2 1
"Schwann cells", a historical landmark in neurology 1
A novel NF1 gene mutation in an Italian family with neurofibromatosis type 1. 1
BRAIN-DERIVED NEUROTROPHIC FACTOR (BDNF) GENE IN RELAPSING-REMITTING MULTIPLE SCLEROSIS (RRMS): LONGITUDINAL EVALUATION 1
Individual differences in depression are associated with abnormal function of the limbic system in multiple sclerosis patients. 1
Acute levodopa and ropinirolo tests in Parkinson s disease 1
Color vision inpatients with Parkinson disease. Usefulness of three pseudoisochromatic tests 1
Compound heterozygosity in DJ-1 gene non-coding portion related to parkinsonism. 1
Genetic study of SCN1A-related epilepsies in southern Italy. 1
A new MR imaging index for differentiation of progressive supranuclear palsy-parkinsonism from Parkinson's disease. 1
Alpha-synuclein promoter haplotypes and dementia in Parkinson s disease . 1
Reply to: "Experience with a New Index to Differentiate Parkinson's Disease and Progressive Supranuclear Pals 1
'The syphilitic' by Albrecht Dürer (1471-1528). 1
Casimir Funk: His discovery of the vitamins and their deficiency disorders 1
Increased glutamate + glutamine levels in the thalamus of patients with essential tremor: A preliminary proton MR spectroscopic study 1
Video-oculographic biomarkers for evaluating vertical ocular dysfunction in progressive supranuclear palsy 1
Empty sella and bilateral transverse sinus stenosis predict raised intracranial pressure in the absence of papilloedema: a preliminary study. 1
Cerebellar voxel-based morphometry in essential tremor 1
Refining initial diagnosis of Parkinson's disease after follow-up: A 4-year prospective clinical and magnetic resonance imaging study 1
Tractography in Amyotrophic Lateral Sclerosis using a novel probabilistic tool: a study with tract-based reconstruction compared to voxel-based approach 1
A novel mutation in FKRP gene in Italian patient with LGMD. 1
A simple method for diagnosis of autosomal recessive spinal muscular atrophy by denaturing high-performance liquid chromatography 1
ANALISI CLINICO-GENETICA IN UNA FAMIGLIA ITALIANA CON ATASSIA SPINOCEREBELLARE AUTOSOMICO-DOMINANTE 1
Thalamic neurometabolic alterations in tremulous Parkinson's disease: A preliminary proton MR spectroscopy study. 1
Association between Synapsin III gene promoter polymorphisms and multiple sclerosis 1
A novel exon 1 mutation in a patient with atypical lafora progressive myoclonus epilepsy seen as childhood-onset cognitive deficit. 1
Corticospinal tract abnormalities and ventricular dilatation: A transdiagnostic comparative tractography study 1
Color Vision in Medicine 1
Cerebellar atrophy in Essential tremor using automated segmentation method. 1
Magnetic Resonance Support Vector Machine Discriminates Between Parkinson Disease and Progressive Supranuclear Palsy 1
Adaptive cortical changes and the functional correlates of visuo-motor integration in relapsing-remitting multiple sclerosis 1
A large family with pure autosomal dominant hereditary spastic paraplegia from southern Italy mapping to chromosome 14q11.2-q24.3. 1
A new CHCHD2 mutation identified in a southern italy patient with multiple system atrophy 1
Structural connectivity differences in essential tremor with and without resting tremor. 1
: Posture-related cough headache and orthostatic drop in lumbar CSF pressure. 1
Intracellular FMRpolyG-Hsp70 complex in fibroblast cells from a patient affected by fragile X tremor ataxia syndrome 1
REM-Sleep Behavior Disorder in Patients With Essential Tremor: What Is Its Clinical Significance? 1
Administration of levodopa modulates the neural and behavioural response associated with cognitive interference in PD patients 1
Electrophysiological and structural MRI correlates of dystonic head rotation in drug-naive patients with torticollis 1
A novel CAPN3 gene mutation in a LGMD patient from Southern Italy 1
Evolving Cellular Neural Networks for the Automated Segmentation of Multiple Sclerosis Lesions 1
Brain atrophy evolution and lesion load accrual in multiple sclerosis: a 2-year follow-up study 1
Voxel-based morphometry to detect effect of APOE on brain gray matter changes in Parkinson's Disease. 1
The neuroanatomical correlates of anxiety in a healthy population: differences between the State-Trait Anxiety 1 Inventory and the Hamilton Anxiety Rating Scale 1
Automatic Detection of White Matter Hyperintensities in Healthy Aging and Pathology Using Magnetic Resonance Imaging: A Review. 1
Multimodal assessment of normal-appearing corpus callosum is a useful marker of disability in relapsing-remitting multiple sclerosis: an MRI cluster analysis study 1
Dopaminergic modulation of cognitive interference after pharmacological washout in Parkinson s disease 1
Dopaminergic modulation of cognitive interference after pharmacological washout in parkinson's disease 1
The corticospinal tract profile in amyotrophic lateral sclerosis. 1
Three novel SCN1A missense mutations in generalized epilepsy with febrile seizures plus 1
Was the subject portrayed in "A Man" by Cornelis Anthonisz around 1530 really affected by progressive supranuclear palsy? 1
Fully automated segmentation of the pons and midbrain using human T1 MR brain images 1
Blink reflex recovery cycle in patients with essential tremor associated with resting tremor. 1
Cortical atrophy distinguishes idiopathic normal-pressure hydrocephalus from progressive supranuclear palsy: A machine learning approach 1
Hans Berger: father of electroencephalography 1
Association between Synapsin III gene promoter polymorphisms and multiple sclerosis. 1
Brain atrophy and lesion load in a large population of patients with multiple sclerosis. 1
The relationship between regional microstructural abnormalities of the corpus callosum and physical and cognitive disability in relapsing-remitting multiple sclerosis 1
Dysfunctions within limbic-motor networks in amyotrophic lateral sclerosis 1
Identificazione di una nuova mutazione nel gene OPA1 in una famiglia affetta da atrofia ottica e sordità. 1
Diagnostic Accuracy of Magnetic Resonance Imaging Measures of Brain Atrophy Across the Spectrum of Progressive Supranuclear Palsy and Corticobasal Degeneration 1
A comprehensive mutation analysis of PINK1 gene in South Italy patients with early and late onset Parkinsonism. 1
A novel locus for Autosomal Dominant Distal Motor Neuronopathy maps to chromosome 4q-ter 1
Totale 129
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Categoria #
all - tutte 5.778
article - articoli 4.092
book - libri 8
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 17
Totale 9.895
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2023/2024133 0 0 0 0 0 0 0 0 11 0 83 39
2024/20254 4 0 0 0 0 0 0 0 0 0 0 0
Totale 137